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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808104Generated: November 1, 2026

1-Bromonaphthalene → 1-Cyclopropylnaphthalene

https://huagongshe.com/reaction/1808104

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromonaphthaleneHCID 7001—
ReactantHCID 178418630HCID 178418630—
CatalystHCID 178418745HCID 178418745—
SolventTetrahydrofuranHCID 8028—
Product1-CyclopropylnaphthaleneHCID 1466869376%

Reaction Conditions

Temperature0 °C

Reaction Steps

Cyclopropylmagnesium bromide (150 mL, 0.5M in tetrahydrofuran) was slowly added to a solution of 1-bromonaphthalene (10 g, 50 mmol) and [1,3-bis(diphenylphosphino)propane]dichloro nickel (II) in tetrahydrofuran (10 mL) stirred at 0° C., and the reaction mixture stirred at room temperature for 16 hours. The solvent was removed under reduced pressure and ethyl acetate and aqueous ammonium chloride were added. After extraction, the organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography to yield 1-cyclopropylnaphthalene (6.4 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357713B2
Source datasetuspto-grants-2013_01
ORD IDord-542523701cf4434196a48fee7bd78211
Source noteuspto-grants-2013_01